| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24136317-24136398 | Common:1; Rare:19 | ||||
| chr14:24141562-24141862 | Common:1; Rare:67 | ||||
| chr14:24146587-24146693 | Rare:40 | ||||
| chr14:24147212-24147655 | Common:4; Rare:113 | ||||
| chr14:24171759-24172119 | Common:5; Rare:85 | ||||
| chr14:24195393-24195746 | Common:2; Rare:77 | ||||
| chr14:24213049-24213205 | Rare:29 | ||||
| chr14:24213421-24213529 | Rare:38 | ||||
| chr14:24213531-24213664 | Common:3; Rare:38 | ||||
| chr14:24215939-24216037 | Common:1; Rare:41 | ||||
| chr14:24216043-24216122 | Rare:20 | ||||
| chr14:24232248-24232707 | Common:8; Rare:116 | ||||
| chr14:24232776-24232954 | Common:1; Rare:38 | ||||
| chr14:24242272-24242433 | Rare:52; Clinvar (benign):2 | ||||
| chr14:24242561-24242770 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):2 |